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FOXI1 抗体

This anti-FOXI1 antibody is a 兔 多克隆 antibody detecting FOXI1 in WB 和 ELISA. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN2458351
发货至: 中国

Quick Overview for FOXI1 抗体 (ABIN2458351)

抗原

See all FOXI1 抗体
FOXI1 (Forkhead Box I1 (FOXI1))

适用

  • 49
  • 9
  • 6
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  • 5
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  • 3
  • 2
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 43
  • 5
  • 1

克隆类型

  • 46
  • 3
多克隆

标记

  • 26
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FOXI1 antibody is un-conjugated

应用范围

  • 29
  • 19
  • 13
  • 13
  • 9
  • 7
  • 4
  • 3
  • 3
  • 3
  • 1
Western Blotting (WB), ELISA
  • 纯化方法

    Antibody is purified by peptide affinity chromatography method.

    免疫原

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FOXI1.
  • 应用备注

    FOXI1 antibody can be used for detection of FOXI1 by ELISA at 1:62500. FOXI1 antibody can be used for detection of FOXI1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    浓度

    1 mg/mL

    缓冲液

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    注意事项

    As with any antibody avoid repeat freeze-thaw cycles.

    储存条件

    4 °C/-20 °C

    储存方法

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store FOXI1 antibody at -20 °C.
  • 抗原

    FOXI1 (Forkhead Box I1 (FOXI1))

    别名

    FOXI1

    背景

    FOXI1 belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. FOXI1 may plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis.This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined, however, it is possible that this gene plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis. Mutations in this gene may be associated with the common cavity phenotype. Two transcript variants encoding different isoforms have been found for this gene.

    分子量

    41 kDa

    基因ID

    2299

    NCBI登录号

    NP_036320

    UniProt

    Q12951
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